Immunosuppressed organ allograft recipients have a 3- to 4-fold increased r
isk of developing tumours, but the risk of developing certain cancers is in
creased several hundredfold. With the exception of skin and lip cancers, mo
st of the common malignancies seen in the general population are not increa
sed in incidence. Instead, there is a higher frequency of some relatively r
are tumours, including post-transplant lymphomas and lymphoproliferative di
sorders (PTLD), Kaposi's sarcoma (KS), renal carcinomas, in situ carcinomas
of the uterine cervix, hepatobiliary carcinomas, anogenital carcinomas and
various sarcomas (excluding KS). Skin and lip cancers present some unusual
features: a remarkable frequency of KS, reversal of the ratio of basal to
squamous cell carcinomas seen in the general population, the young age of t
he patients, and the high incidence of multiple rumours (in 43% of the pati
ents). Anogenital cancers occur at a much younger age than in the general p
opulation. Salient features of PTLD are the high frequency of Epstein-Barr
virus-related lesions, frequent involvement of extranodal sites, a marked p
redilection for the brain and frequent allograft involvement.
As the immunosuppressed state per se and various potentially oncogenic viru
ses play a major role in causing these cancers, preventative measures inclu
de reducing immunosuppression to the lowest level compatible with good allo
graft function and prophylactic measures against certain virus infections.
Reduction of exposure to sunlight may also decrease the incidence of skin c
ancer. In addition to conventional treatments (resection. radiation therapy
, chemotherapy) patients may receive antiviral drugs, interferon-alpha and
various other manipulations of the immune system. A significant percentage
of cases of PTLD and KS respond to reduction or cessation of immunosuppress
ive therapy.